Canonical Allele Identifier: CA343776885

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657792931
• gnomAD v3: 1-173912014-C-T
• gnomAD v4: 1-173912014-C-T
• MyVariant Identifiers: chr1:g.173881152C>T (hg19) ; chr1:g.173912014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173912014C>T , CM000663.2:g.173912014C>T	GRCh38
NC_000001.10:g.173881152C>T , CM000663.1:g.173881152C>T	GRCh37
NC_000001.9:g.172147775C>T	NCBI36
NG_012462.1:g.10365G>A , LRG_577:g.10365G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.409G>A MANE Select	ENSP00000356671.3:p.Val137Ile
ENST00000367698.3:c.409G>A	ENSP00000356671.3:p.Val137Ile
ENST00000487183.1:n.114G>A
ENST00000494024.1:n.635G>A
ENST00000617423.4:c.409G>A	ENSP00000478688.1:p.Val137Ile
NM_000488.3:c.409G>A , LRG_577t1:c.409G>A	NP_000479.1:p.Val137Ile
XM_005245198.2:c.265G>A	XP_005245255.1:p.Val89Ile
NM_001365052.1:c.265G>A	NP_001351981.1:p.Val89Ile
NM_000488.4:c.409G>A MANE Select	NP_000479.1:p.Val137Ile
NM_001365052.2:c.265G>A	NP_001351981.1:p.Val89Ile
NM_001386302.1:c.409G>A	NP_001373231.1:p.Val137Ile
NM_001386303.1:c.490G>A	NP_001373232.1:p.Val164Ile
NM_001386304.1:c.409G>A	NP_001373233.1:p.Val137Ile
NM_001386305.1:c.409G>A	NP_001373234.1:p.Val137Ile
NM_001386306.1:c.409-1123G>A	NP_001373235.1:n.409-1123G>A